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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148149copy number variation1nstd102humanPathogenic GRCh38 chr1: 145,822,587-146,064,587 , GRCh37.p13 chr1|NW_003871055.3: 2,638,000-2,880,000 , GRCh37.p13 chr1: 145,370,415-145,612,526 TXNIP, PEX11B, 22 more genes
    nsv7148064copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,365,275-145,826,979 , GRCh38.p12 chr1: 145,608,084-146,069,727 ANKRD34A, RNVU1-6, 26 more genes
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7098839copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123 CCT8P1, LINC01719, 120 more genes
    nsv7098724copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371217, 150 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7045394inversion1nstd229human GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1|NW_003871055.3: 547,587-4,154,677 , MIR6736, 130 more genes
    nsv6636744copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,493,131-147,831,043 , GRCh38.p12 chr1: 145,430,980-148,358,916 PDZK1, ANKRD34A, 102 more genes
    nsv6634386copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,626,685-147,597,284 , GRCh38.p12 chr1: 145,430,980-148,125,001 LOC391092, NBPF10, 84 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6333880copy number variation1nstd223human GRCh38 chr1: 145,488,103-148,061,210 , GRCh37.p13 chr1|NW_003871055.3: 2,303,516-4,876,623 , TRR-CCT6-2, 79 more genes
    nsv6290494copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,369,199-145,886,340 , GRCh38.p12 chr1: 145,601,946-146,065,803 POLR3GL, TXNIP, 26 more genes
    nsv6290404copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,043,714-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211 , TRN-GTT9-2, 150 more genes
    nsv6290221copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,324,298-146,018,577 , GRCh38.p12 chr1: 145,601,946-146,113,874 RBM8A, POLR3C, 26 more genes
    nsv6290073copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,824,148-149,378,266 , BCL9, 215 more genes
    nsv6290071copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,806,599-149,209,289 , BCL9, 215 more genes
    nsv6289910copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr1|NW_003871055.3: 2,417,359-5,412,838 , GRCh38 chr1: 145,601,946-148,597,425 BCL9, FMO5, 110 more genes
    nsv6139080copy number variation1nstd206human GRCh38 chr1: 146,136,587-146,143,650 , GRCh37.p13 chr1|NW_003871055.3: 2,952,000-2,959,063 , GRCh37.p13 chr1: 145,294,525-145,301,588 NBPF10
    nsv6138813copy number variation1nstd206human GRCh38 chr1: 144,966,587-146,310,000 , GRCh37.p13 chr1|NW_003871055.3: 1,782,000-3,125,413 , NUDT17, 56 more genes
    nsv6138546copy number variation1nstd206human GRCh38 chr1: 146,068,587-146,148,215 , GRCh37.p13 chr1|NW_003871055.3: 2,884,000-2,963,628 , GRCh37.p13 chr1: 145,289,961-145,366,415 NBPF10
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